This is nice You may run into some problems at your first step, because it is a secondary carbon, but you could also use a Heck reaction with Pd(OAc)2 , which is not basic, or an addition to acetone, which would actually leave a functional group in the right place. you just need to write up a description and reference any sources. Bruce Bondurant Roderick Henderson
A condensation reaction into an nucleophile of aldehyde. The dimethyl pyridine reacts as a base in solvent Toluene. The NaOCH3 in Ch3OH is to restore at least one acid group. With the carboxylic acid, the cis isomer. Benzenethiol is the catalyst yeilds with DMF which is a polar solvent. The SOCL2 replaces the hydroxy from the carboxyllic acid with the Chlorine in order to prepare to react with the alkynalcohol Then you use fisher essterfiction.
This is nice You may run into some problems at your first step, because it is a secondary carbon, but you could also use a Heck
reaction with Pd(OAc)2 , which is not basic, or an addition to acetone, which would actually leave
a functional group in the right place. you just need to write up a description and reference any sources.
Bruce Bondurant
Roderick Henderson
Kinorene
http://www.facebook.com/?ref=home#!/photo.php?fbid=10150105549791351&set=a.10150105549786351.314739.614001350
A condensation reaction into an nucleophile of aldehyde. The dimethyl pyridine reacts as a base in solvent Toluene. The NaOCH3 in Ch3OH is to restore at least one acid group. With the carboxylic acid, the cis isomer. Benzenethiol is the catalyst yeilds with DMF which is a polar solvent. The SOCL2 replaces the hydroxy from the carboxyllic acid with the Chlorine in order to prepare to react with the alkynalcohol Then you use fisher essterfiction.